Job Summary
We have an exciting role in our global regulatory organization for a leadership position in our Health Sciences business, which is the global leading probiotics dietary supplement business (originally Danisco and DuPont, now IFF). We are aggressively developing new areas of innovation and expanding our portfolio and our geographic offerings. The successful candidate will collaborate with internal business partners including R&D, Quality, Commercial and Marketing, and Legal in providing governance and interpretation of relevant global regulations concerning dietary/food supplements for a variety of markets. The candidate will also be responsible for partnering with Health Sciences leadership to refresh and implement a global strategy for the GRA team and to build core competencies within the GRA team to enable successful execution. The candidate will also play an important role to represent IFF within trade association and industry meetings, and engage with appropriate Regulatory authorities.
Key Responsibilities:
- Lead and mentor a global GRA team responsible for understanding and implementing regional regulatory strategies.
- Develop and deliver innovative regulatory strategies for existing products and new projects.
- Collaborate closely with IFF Health Sciences R&D, Quality, Commercial Applications, Manufacturing, and Marketing functions to define optimal regulatory pathways.
- Engage with new projects and product developments, defining regulatory strategies globally and supporting dossier work as needed.
- Provide expertise and insight for the existing product portfolio, leading lifecycle management of product registrations worldwide.
- Ensure relevant risk evaluation and management processes are followed and completed.
- Identify advocacy needs and partner with colleagues globally to track and assess the impact of regulatory developments.
- Engage with competent authorities and trade associations to advocate for regulatory issues impacting IFF's probiotics and dietary enzyme portfolios.
- Translate regulatory issues to relevant internal stakeholders.
- Support dossier development and regulatory agency correspondence.
- Partner with the Clinical Science team to design appropriate clinical trials.
- Provide active customer support on regulatory matters.
We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability.
Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more
What We Do
Meet IFF:
We boldly bring together science and creativity to create what the world needs.
An industry leader in food, beverage, health and biosciences, we create essential solutions – from global icons to unexpected innovations and experiences. Equal parts outspoken and analytical, our international collective of thinkers working with customers to bring scents, tastes, experiences, ingredients and solutions for products people crave.
With 24,000 employees across 65 countries, more than 110 manufacturing facilities, 100 R&D centers, and 33,000 customers across the world, we’re poised to make a difference on an unprecedented scale. Without our boundary-pushing passion and end-to-end expertise, the future wouldn’t be the same.
Visit us at www.iff.com to learn more about how our talented people and new technology are challenging the expected, championing creators and doing more good for people and planet.
Explore what sets us apart.
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